Nyiri Zoltán, Novák Márton, Bodai Zsolt, Szabó Bálint Sámuel, Eke Zsuzsanna, Záray Gyula, Szigeti Tamás
Joint Research and Training Laboratory on Separation Techniques, Institute of Chemistry, Eötvös Loránd University, Pázmány Péter stny. 1/A, H-1117 Budapest, Hungary.
Joint Research and Training Laboratory on Separation Techniques, Institute of Chemistry, Eötvös Loránd University, Pázmány Péter stny. 1/A, H-1117 Budapest, Hungary; Wessling International Research and Educational Center, Fóti út 56, H-1047 Budapest, Hungary.
J Chromatogr A. 2016 Nov 11;1472:88-98. doi: 10.1016/j.chroma.2016.10.021. Epub 2016 Oct 13.
An analytical method has been developed for the quantitative determination of polycyclic aromatic hydrocarbons (PAHs) and their nitrated and oxygenated derivatives (nitro- and oxy-PAHs respectively) in particulate matter (PM) samples. The sample preparation procedure included only a simple and quick sonication-assisted extraction step, clean-up based on addition of water and centrifugation as well as pre-concentration under N stream. The determination of 16 PAHs and 4 oxy-PAHs was carried out by gas chromatography-mass spectrometry, while liquid chromatography-tandem mass spectrometry was used in the case of the 11 investigated nitro-PAHs. The optimized method was fully evaluated in terms of trueness, precision (repeatability), limit of detection (LOD), limit of quantification (LOQ), sensitivity and linearity. The LOQ values ranged at pgm level for the investigated PAHs (42pgm), oxy-PAHs (either 42 or 83pgm) and nitro-PAHs (either 83 or 167pgm) as well. The developed method was applied for the quantitative determination of PAHs, nitro- and oxy-PAHs in urban PM (particles with aerodynamic diameter smaller than 2.5μm) samples (n=36) collected in Budapest, Hungary. Almost 100% of the PM samples contained the investigated PAHs and oxy-PAHs in detectable and quantifiable amounts; however, the concentration of the nitro-PAHs was generally lower than the corresponding LOD/LOQ values. According to our results, during the 3-year long sampling campaign the concentration of benzo(a)pyrene never exceeded the limit value (1ngm) set by the European Commission.
已开发出一种分析方法,用于定量测定颗粒物(PM)样品中的多环芳烃(PAHs)及其硝化和氧化衍生物(分别为硝基-PAHs和氧代-PAHs)。样品制备程序仅包括一个简单快速的超声辅助萃取步骤、基于加水和离心的净化以及在氮气流下的预浓缩。通过气相色谱-质谱法测定16种PAHs和4种氧代-PAHs,而对于11种研究的硝基-PAHs则使用液相色谱-串联质谱法。从准确性、精密度(重复性)、检测限(LOD)、定量限(LOQ)、灵敏度和线性等方面对优化后的方法进行了全面评估。所研究的PAHs(42pgm)、氧代-PAHs(42或83pgm)和硝基-PAHs(83或167pgm)的LOQ值均在皮克/克水平。所开发的方法用于定量测定在匈牙利布达佩斯采集的城市PM(空气动力学直径小于2.5μm的颗粒)样品(n = 36)中的PAHs、硝基-PAHs和氧代-PAHs。几乎100%的PM样品中含有可检测和可定量的所研究的PAHs和氧代-PAHs;然而,硝基-PAHs的浓度通常低于相应的LOD/LOQ值。根据我们的结果,在为期3年的采样活动中,苯并(a)芘的浓度从未超过欧盟委员会设定的限值(1ngm)。